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Intravenous metoclopramide to improve the success rate of blind bedside post-pyloric placement of feeding tube in pediatric critically ill patients: A randomized, double-blind, placebo-controlled study

Intravenous metoclopramide to improve the success rate of blind bedside post-pyloric placement of feeding tube in pediatric critically ill patients: A randomized, double-blind, placebo-controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190821002
Enrollment
100
Registered
2019-08-21
Start date
2018-12-28
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critically ill patient Metoclopramide&#44

Interventions

case &#45
metroclopramide infusion 30 mins before placement of feeding tube ,control &#45
NSS infusion 30 mins before placement of feeding tube
Experimental Drug,Placebo Comparator Drug
Metoclopramide,Normal saline

Sponsors

Faculty of Medicine Ramathibodi Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Months to 19 Years

Inclusion criteria

Inclusion criteria: - Age of 1 month -19 years - Severe gastroesophageal reflex disease - Feeding intolerance - Decrease or absent gag reflex - Risk of aspiration pneumonia

Exclusion criteria

Exclusion criteria: - Had percutaneous gastric feeding tube - Malrotation of internal abdominal organ - Active bleeding of esophageal varices - Undergo major abdominal surgery - Allergic to metoclopramide

Design outcomes

Primary

MeasureTime frame
The successful rate of blind bedside post-pyloric placement of feeding tube 6-8 hr after placement of feeding tube SPSS—

Secondary

MeasureTime frame
none none none—

Countries

Thailand

Contacts

Public ContactSirima Ketsuwan

Ramathibodi Hospital

sirima_be@hotmail.com086-4116545

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026